Variant #0000259447 (NC_000017.10:g.19552312C>G, NM_000382.2:c.28C>G (ALDH3A2))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.19552312C>G |
DNA change (hg38) |
g.19648999C>G |
Published as |
ALDH3A2(NM_000382.2):c.28C>G (p.(Gln10Glu)), ALDH3A2(NM_000382.3):c.28C>G (p.Q10E), ALDH3A2(NM_001031806.2):c.28C>G (p.Q10E) |
ISCN |
- |
DB-ID |
ALDH3A2_000089 See all 3 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.0036 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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